Product Recalls in Alaska
Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,463 recalls have been distributed to Alaska in the last 12 months.
Showing 14281–14300 of 27,254 recalls
Recalled Item: PROXIMATE¿ PPH Hemorrhoidal Circular Stapler Product Code:PPH03 PPH03: The...
The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROXIMATE¿ HCS Hemorrhoidal Circular Stapler Product Code: PPH01 PPH01: The...
The Issue: Hemorrhoidal Circular Stapler may have been assembled without a washer, this...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: I-View¿ Contrast Enhanced Digital Mammography Recalled by Hologic, Inc. Due...
The Issue: Calibration issue not possible to visualize contrast uptake in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vygon DUALSTOP Red Cap used for intravascular lines Product Code: Recalled...
The Issue: DualStop Caps defect causing leaks in affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD SureStep Foley Tray System Bardex I.C. Complete Care Temperature...
The Issue: Some SureStep" Foley Tray Systems with product catalog number A319418AM and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vyon DUALSTOP White Cap used for intravascular lines Product Code: Recalled...
The Issue: DualStop Caps defect causing leaks in affected product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VisuMax Software Version 2.10.13 with activated Software-Module ReLEx...
The Issue: VisuMax devices with software version 2.10.13 and activated SW-Module ReLEx...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Adapter Percutaneous Pin Recalled by Medtronic Navigation, Inc....
The Issue: Under certain circumstances, the percutaneous pin adapter used with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The UniCel DxI 600 and 800 Access Immunoassay Systems Recalled by Beckman...
The Issue: When racks are front-loaded onto the sample presentation unit while samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breast Milk Transfer Lid for use with Oral Syringe Connectors Model:...
The Issue: The sterility may be compromised due to a potential breach in the packaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Toothete Oral Care Sodium Bicarbonate Mouthpaste Recalled by Sage Products...
The Issue: A voluntary recall of a lot (67924) of Independent Care System due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxC 660i Recalled by Beckman Coulter Inc. Due to When racks are...
The Issue: When racks are front-loaded onto the sample presentation unit while samples...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equinoxe Preserve Humeral Stem Recalled by Exactech, Inc. Due to Possibility...
The Issue: Possibility that the Equinoxe Preserve Humeral Stem, 8mm, was inadvertently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DX-D 600 DIRECT RADIOGRAPHY SYSTEM Product Usage: The DX-D 600 Recalled by...
The Issue: After an upgrade of the software of the Overhead Tube Crane, there were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triton Sponge System (Software) Recalled by Stryker Instruments Div. of...
The Issue: Gauss Surgical is updating the Instructions for Use (IFU) for our Triton...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Total Knee Replacement System Recalled by Conformis, Inc. Due to...
The Issue: The kits were prepared with incorrect patient ID labels and may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C2 CryoBalloon Controller Recalled by PENTAX of America Inc Due to The...
The Issue: The Controller does not detect overpressure in the balloon during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion lnterventional Fluoroscopic X-ray System Recalled by Philips Medical...
The Issue: Philips has discovered through customer complaints and internal testing an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Visitec Soft Tip Cannula Recalled by Beaver Visitec Due to Certain lots...
The Issue: Certain lots are missing a protective sheath component over the silicone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Biograph Horizon PET/CT System Recalled by Siemens Medical Solutions...
The Issue: Improper design or specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.